BA 40501 XL (UDI 08682495018665)
Manufactured by BİOAKTİF TIBBİ ÜRÜNLER VE TEKNİK TEKSTİL SAN. TİC. LTD. ŞTİ.
Device Regulatory Overview
The BA 40501 XL (Model/Catalog Number: BA 40501 XL) is a medical device manufactured by BİOAKTİF TIBBİ ÜRÜNLER VE TEKNİK TEKSTİL SAN. TİC. LTD. ŞTİ.. This product is indexed under FDA Product Code / Category Classification Y06120601 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- BA 40501 XL
- Product Code / EMDN
- Y06120601
- Device Name
- FOOT HEALTH SUPPORT PRODUCTS
- Database Sync Date
- 2026-08-09 16:30:06
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of BA 40501 XL?
The registered manufacturer of record for BA 40501 XL is BİOAKTİF TIBBİ ÜRÜNLER VE TEKNİK TEKSTİL SAN. TİC. LTD. ŞTİ..
What is the Primary UDI-DI identifier for BA 40501 XL?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08682495018665.
What classification code is assigned to this device?
This device is registered under product classification code Y06120601.
Similar Classification Devices (Y06120601)
Other Devices by BİOAKTİF TIBBİ ÜRÜNLER VE TEKNİK TEKSTİL SAN. TİC. LTD. ŞTİ.
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